溶剂化
电解质
电化学窗口
化学工程
电化学
阳极
离子电导率
枝晶(数学)
无机化学
材料科学
吸附
水溶液
电导率
离子液体
化学
电极
离子键合
多孔性
溶剂化壳
聚乙烯吡咯烷酮
壳聚糖
基质(水族馆)
锂(药物)
作者
Xinyuan Bai,Yapeng He,Jianming Feng,Lifeng Yan
出处
期刊:Chemsuschem
[Wiley]
日期:2026-04-18
卷期号:19 (8): e202502451-e202502451
标识
DOI:10.1002/cssc.202502451
摘要
Rechargeable aqueous zinc–iodine (Zn–I 2 ) batteries are promising due to their eco‐friendliness and low cost. However, challenges such as Zn dendrite growth, anode corrosion, and polyiodide shuttling in electrolytes persist. Here, chitosan and agar hydrogel has been prepared as electrolyte, in which the hydrophilic groups in polymers form solvation structure of Zn 2+ . Due to the minimal water content in the system, ClO 4 − also participates in the Zn 2+ solvation structure, further reducing the number of solvated water molecules. Notably, the resulting hydrogel exhibits low water content yet achieves higher ionic conductivity (26.62 mS cm −1 ) than typical water‐poor gels. The reduced activity of H 2 O suppresses Zn dendrite growth and corrosion, significantly extending the electrochemical window to 3.02 V. The assembled Zn||Zn symmetric cells demonstrate exceptional electrochemical stability, operating for over 4000 h at 1 mA cm −2 . For the iodine cathode, elemental iodine is fully adsorbed onto the carbon host. The layered porous structure of the electrode considerably increases its surface area, providing more active sites to facilitate electron transfer and ion diffusion. This, along with uniform iodine dispersion, enhances the practical iodine reaction ratio, yielding a high specific capacity of 186.5 mAh g −1 at 5 A g −1 .
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